Latest News & Updates

Welcome to the Taylored Consultancy Blog where we talk all things Regulatory Affairs, MDR, and legislation for the UK and EU.

Jen Bradburn Jen Bradburn

Key Rules for Marketing Medical Devices

Marketing medical devices can be a challenge. The Advertising Standards Authority (ASA) and Committee of Advertising Practice (CAP) shape the rules for advertising in the UK, including what you can and cannot say about medical devices.

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Bethany Dean Bethany Dean

A Basic Guide to Importing Food Supplements into the UK

Since Brexit, importing goods into Great Britain has completely changed bringing with it a labyrinth of new regulations and standards impacting the smooth operation of businesses dealing in dietary supplements, food supplement, vitamins, and other nutrition-focused products.

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Bethany Dean Bethany Dean

What is the role of a UKRP?

Medical device registrations and regulations are ever evolving so understanding how a UKRP can help has become a really important part of post-Brexit processes.

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Bethany Dean Bethany Dean

A Quick Look at Medical Device Regulations in the UK

The UK's regulatory environment for medical devices has evolved over the years. Historically, we followed the European Union's Medical Device Directive (MDD). However, post-Brexit, we have established our own regulatory system.

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Bethany Dean Bethany Dean

Food Supplement Labelling

In the bustling world of health and wellness, food supplements have become an integral part of many individuals' daily routines. Whether it's bolstering essential nutrients or supporting specific health goals, the demand for these products continues to soar.

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Bethany Dean Bethany Dean

UK Responsible Person

In the landscape of consumer safety and regulatory compliance, the UK Responsible Person plays a pivotal role in ensuring that products placed on the market meet the necessary standards and requirements.

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